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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Pyrido[4,3-d]pyrimidin-4(3H)-one, 5,7-dichloro-

Clc1nc(Cl)cc2c1c(=O)[nH]cn2 Request for Quotation
Chemical Name: Pyrido[4,3-d]pyrimidin-4(3H)-one, 5,7-dichloro-
CAS Number: 918898-11-0
Product Number: AG00H2WZ(AGN-PC-0ON0MA)
Synonyms:
MDL No:
Molecular Formula: C7H3Cl2N3O
Molecular Weight: 216.0242

Identification/Properties

Properties
Storage:
2-8℃;Inert atmosphere;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5,7-Dichloropyrido[4,3-d]pyrimidin-4(3H)-one is a versatile compound widely utilized in chemical synthesis processes. Its unique structure and reactivity make it a valuable building block for the creation of various functional molecules in the field of organic chemistry.One of the key applications of 5,7-Dichloropyrido[4,3-d]pyrimidin-4(3H)-one is its role as a precursor in the synthesis of pharmaceutical compounds. This compound serves as a crucial intermediate in the production of potential drug candidates due to its ability to undergo different chemical transformations, such as substitution reactions and cyclization reactions. By incorporating 5,7-Dichloropyrido[4,3-d]pyrimidin-4(3H)-one into the synthesis route, chemists can access diverse structural motifs and functional groups needed for the development of new drugs with enhanced bioactivity and pharmacokinetic properties.Furthermore, 5,7-Dichloropyrido[4,3-d]pyrimidin-4(3H)-one is also employed in the preparation of agrochemicals and specialty chemicals. Its selective reactivity and compatibility with various synthetic methodologies enable the efficient construction of molecular scaffolds with desirable properties for agricultural applications and other industrial purposes. Through strategic manipulation of its chemical structure, researchers can tailor the properties of the resulting compounds to meet specific requirements in terms of efficacy, stability, and environmental impact.